Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,665 recalls have been distributed to North Dakota in the last 12 months.
Showing 43501–43520 of 47,938 recalls
Recalled Item: See's Dark Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...
The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: See's Milk Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...
The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prednisone Tablet USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: Labeling: Missing Label; missing label on blister card
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by CareFusion 213, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility; Immediate product pouches may not be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Infinia Hawkeye 4 Option For Dual-Head Variable Angle Gamma...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima NM/CT 640 Product Usage: The GE Optima NM/CT 640 Recalled by GE...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to GE became aware of...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Affirm VPIII Microbial Identification Tests Recalled by Becton Dickinson...
The Issue: In vitro diagnostic test kit may exhibit invalid internal negative control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...
The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...
The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...
The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TBIL Slides packaged as 300 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PROT Slides packaged as 90 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products SALI Slides packaged as 90 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products ALKP Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHOS Slides packaged as 300 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.